Datoteka:Hutchinson-Gilford Progeria Syndrome.png

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Opis Hutchinson-Gilford Progeria Syndrome. HGPS is a childhood disorder caused by mutations in one of the major architectural proteins of the cell nucleus. In HGPS patients the cell nucleus has dramatically aberrant morphology (bottom, right) rather than the uniform shape typically found in healthy individuals (top, right).
Datum Published: November 15, 2005
Izvor The Cell Nucleus and Aging: Tantalizing Clues and Hopeful Promises. Scaffidi P, Gordon L, Misteli T. PLoS Biology Vol. 3/11/2005, e395 doi:10.1371/journal.pbio.0030395
Autor See Source
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Datum/vrijemeSmanjeni pregledDimenzijeKorisnikKomentar
trenutno20:44, 4 decembar 2006Smanjeni pregled verzije na dan 20:44, 4 decembar 20061.200 × 968 (1,09 MB)Ayacop{{Information |Description='''Hutchinson-Gilford Progeria Syndrome.''' HGPS is a childhood disorder caused by mutations in one of the major architectural proteins of the cell nucleus. In HGPS patients the cell nucleus has dramatically aberrant morphology

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